ENST00000324071.10:c.1189C>A
MANE Select
|
ENSP00000324648.2:p.His397Asn
|
|
ENST00000598834.2:c.1176+225C>A
|
|
|
ENST00000324071.8:c.1189C>A
|
ENSP00000324648.2:p.His397Asn
|
|
ENST00000593831.1:c.481C>A
|
ENSP00000470582.1:p.His161Asn
|
|
ENST00000597612.1:n.647+225C>A
|
|
|
NM_000767.4:c.1189C>A
|
NP_000758.1:p.His397Asn
|
|
XM_005258569.3:c.1152+225C>A
|
XP_005258626.1:n.1152+225C>A
|
|
XM_006723050.2:c.1189C>A
|
XP_006723113.1:p.His397Asn
|
|
XM_011526546.1:c.1153-106C>A
|
XP_011524848.1:n.1153-106C>A
|
|
XM_011526547.1:c.1152+225C>A
|
XP_011524849.1:n.1152+225C>A
|
|
XM_011526548.1:c.709C>A
|
XP_011524850.1:p.His237Asn
|
|
XM_011526549.1:c.598C>A
|
XP_011524851.1:p.His200Asn
|
|
XM_011526550.1:c.589C>A
|
XP_011524852.1:p.His197Asn
|
|
NM_000767.5:c.1189C>A
MANE Select
|
NP_000758.1:p.His397Asn
|
|